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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260274Generated: November 1, 2026

Propanedioyl dichloride → 5-(3-Cyanophenyl)-1H-naphtho[1,2-b][1,4]diazepin-2,4(3H,5H)-dione

https://huagongshe.com/reaction/1260274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanedioyl dichlorideHCID 74269—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(1-Amino-2-naphthylamino)benzonitrileHCID 67993912—
SolventTolueneHCID 1140—
Product5-(3-Cyanophenyl)-1H-naphtho[1,2-b][1,4]diazepin-2,4(3H,5H)-dioneHCID 4686321927.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To an ice-cold solution of 3-(1-amino-2-naphthylamino)benzonitrile (968 mg, 3.73 mmol) in toluene (10 mL) was added malonyl chloride (436 μL, 4.48 mmol). The mixture was stirred at 80° C. for 20 minutes, then at 110° C. for 10 minutes. After the reaction mixture was cooled to room temperature, the solution part of the reaction mixture was poured into a saturated aqueous sodium bicarbonate solution, and was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. While The precipitated solid in the reaction mixture was dissolved in chloroform, was washed with a saturated aqueous sodium bicarbonate solution, and saturated brine. After drying over anhydrous sodium sulfate, the solvent was removed under reduced pressure. The residues were combined, and Each product purified by silica gel column chromatography (hexane/ethyl acetate=1/4), and the residue was recrystallized from ethyl acetate to give the titled compound as a pale yellow crystal (335 mg, yield 27%). mp: 220-222° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470814B2
Source datasetuspto-grants-2013_06
ORD IDord-005e2a738d284744bd44c917c56c5f5c
Source noteuspto-grants-2013_06